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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239073생성일: 2026년 10월 24일

Methyl iodide → Ethyl 2-(4-methylphenyl)propanoate

https://huagongshe.com/ko/reaction/239073

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Ethyl p-tolylacetateHCID 84175—
반응물Benzeneacetic acid, alpha-methyl-, ethyl esterHCID 99643—
반응물Lithium diisopropylamideHCID 2724682—
용매TetrahydrofuranHCID 8028—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물Ethyl 2-(4-methylphenyl)propanoateHCID 1107052486%

반응 단계

According to the procedure given for the synthesis of 202, ethyl p-tolylacetate (2.72 g, 15.2 mmol) was reacted with LDA (7.6 mL, 15.25 mmol) and methyl iodide (3.03 g, 21.30 mmol) in anhydrous THF (70 mL) and DMPU (1 mL). After aqueous workup and extraction, the residue was distilled in high vacuo to give 203 (2.5 g, 86.0%) as an oil. Bp 59-63° C./0.2 mmHg. 1H NMR (CDCl3): δ (ppm) 7.18 (d, 2 H, J=8.1), 7.10 (d, 2 H, J=8.1), 4.09 (m, 2 H), 3.67 (q, 1 H, J=7.2), 2.29 (s, 3 H), 1.47 (d, J=7.2 Hz, 3 H), 1.20 (t, J=5.7 Hz, 3 H). 13C NMR (75 MHz, CDCl3/TMS): δ (ppm) 174.71, 137.80, 136.63, 129.33, 129.14, 127.36, 60.66, 45.18, 21.05, 18.70, 14.15.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642653B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-af776805c1c24e9e8a397dbeb88e47ea
출처 메모uspto-grants-2014_02